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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803852Generated: November 1, 2026

Trifluoroacetic acid → HCID 46244494, compound

https://huagongshe.com/reaction/1803852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantTetramethylammonium Triacetoxyborohydride (>90%)HCID 13696215—
ReactantHCID 46244400HCID 46244400—
SolventDichloromethaneHCID 6344—
ProductHCID 46244494HCID 4624449446.5%

Reaction Steps

2-Amino-N-[5-(3,5-difluoro-benzyloxy)-1H-indazol-3-yl]-4-[(3-dimethylamino-propyl)-methyl-amino]-benzamide (150 mg, 0.29 mmol) in DCM (4 mL) was treated, at 4° C., under a nitrogen atmosphere, with tetrahydro-4H-pyran-4-one (0.34 mL, 0.37 mmol), TFA (0.23 mL, 2.95 mmol) and finally with tetramethylammonium triacetoxyborohydride ((204 mg, 0.74 mmol). After 1.5 hours DCM, was added (25 mL) and the organic layer was washed with water (25 mL), saturated NaHCO3 solution (25 mL) and brine. After drying over anhydrous sodium sulfate, removal of the solvent and purification of the crude over silica gel (DCM: 7N NH3 in MeOH 9:1), 80 mg of title compound were obtained in 46% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354399B2
Source datasetuspto-grants-2013_01
ORD IDord-9e154a28d7094433988c9965663bf759
Source noteuspto-grants-2013_01